» Articles » PMID: 38451314

Clinical Evidence for Efficacy of Pembrolizumab in MSI-H and TMB-H Advanced Solid Tumor: Results from Three Cancer Centers in China

Abstract

Background: Pembrolizumab has been indicated in the treatment of solid tumors with high frequency microsatellite instability (MSI-H) or high tumor mutational burden (TMB-H); however, real-world data on the effectiveness of pembrolizumab with or without chemotherapy in this molecular subset remain limited. Our retrospective study evaluated the clinical efficacy and safety of pembrolizumab in treating advanced solid tumors with either MSI-H or TMB-H.

Methods: This retrospective study analyzed data from 116 patients with MSI-H or TMB-H advanced solid cancers who received pembrolizumab with or without chemotherapy regardless of treatment setting. We analyzed objective response rate (ORR) and progression-free survival (PFS).

Results: The top three cancer types were colorectal (48.6% MSI-H, 6.5% TMB-H), lung (15.4% MSI-H, 84.4% TMB-H), and gastric (15.4% MSI-H, 5.1% TMB-H). The ORR with pembrolizumab was 52.6%, including complete response (CR) observed in 8.6% (n = 10) of cases and partial responses (PR) in 43.9% (n = 51). Of the 93 patients who received first-line pembrolizumab, 52 patients achieved objective response (10 CR, 42 PR), with a median PFS of 14.0 months (95% confidence intervals [CI] 6.6-21.4). Of the 23 who received subsequent-line pembrolizumab, the ORR was 39.1%, disease control rate was 91.3%, and median PFS was 5.7 months (95% CI 3.9-7.5). Treatment-related adverse events were observed in 32 patients (27.6%), with no reported treatment-related fatal adverse events.

Conclusion: Our study provides real-world evidence on the clinical effectiveness of pembrolizumab with or without chemotherapy in the treatment of patients with MSI-H and TMB-H advanced solid cancers.

Citing Articles

Biomarkers for the Evaluation of Immunotherapy in Patients with Cholangiocarcinoma.

Bousou T, Sarantis P, Anastasiou I, Trifylli E, Liapopoulos D, Korakaki D Cancers (Basel). 2025; 17(3).

PMID: 39941920 PMC: 11817672. DOI: 10.3390/cancers17030555.


DHX34 as a promising biomarker for prognosis, immunotherapy and chemotherapy in Pan-Cancer: A Comprehensive Analysis and Experimental Validation.

Liu N, Wang Q, Zhu P, He G, Li Z, Chen T J Cancer. 2024; 15(20):6594-6615.

PMID: 39668816 PMC: 11632995. DOI: 10.7150/jca.102230.


The future of cancer treatment: combining radiotherapy with immunotherapy.

Dagar G, Gupta A, Shankar A, Chauhan R, Macha M, Bhat A Front Mol Biosci. 2024; 11:1409300.

PMID: 39044839 PMC: 11263218. DOI: 10.3389/fmolb.2024.1409300.

References
1.
Eso Y, Shimizu T, Takeda H, Takai A, Marusawa H . Microsatellite instability and immune checkpoint inhibitors: toward precision medicine against gastrointestinal and hepatobiliary cancers. J Gastroenterol. 2019; 55(1):15-26. PMC: 6942585. DOI: 10.1007/s00535-019-01620-7. View

2.
Le D, Uram J, Wang H, Bartlett B, Kemberling H, Eyring A . PD-1 Blockade in Tumors with Mismatch-Repair Deficiency. N Engl J Med. 2015; 372(26):2509-20. PMC: 4481136. DOI: 10.1056/NEJMoa1500596. View

3.
Dudley J, Lin M, Le D, Eshleman J . Microsatellite Instability as a Biomarker for PD-1 Blockade. Clin Cancer Res. 2016; 22(4):813-20. DOI: 10.1158/1078-0432.CCR-15-1678. View

4.
Imai K, Yamamoto H . Carcinogenesis and microsatellite instability: the interrelationship between genetics and epigenetics. Carcinogenesis. 2007; 29(4):673-80. DOI: 10.1093/carcin/bgm228. View

5.
Buhard O, Cattaneo F, Wong Y, Yim S, Friedman E, Flejou J . Multipopulation analysis of polymorphisms in five mononucleotide repeats used to determine the microsatellite instability status of human tumors. J Clin Oncol. 2005; 24(2):241-51. DOI: 10.1200/JCO.2005.02.7227. View